Taiwan FDA registration 2f8a190ec9912cb17eb90132438d0017
“Angiomed”LifeStent 5F Vascular Stent System
TW: “安吉美爾德”萊弗史丹血管支架系統
Taiwan·Risk Class 2·MD·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Registered Mar 27, 2023 – Mar 27, 2028ActiveRegistration details
- Analysis ID
- 2f8a190ec9912cb17eb90132438d0017
- License Form
- Ministry of Health Medical Device Import No. 036335
- Customs Code
- DHA05603633506
Company information
- Manufacturer
- ANGIOMED GMBH & CO. MEDIZINTECHNIK KG
- Manufacturer Country
- Germany
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E0001 Cardiovascular stents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 27, 2023
- Expiry Date
- Mar 27, 2028
About this record
Access comprehensive regulatory information for “Angiomed”LifeStent 5F Vascular Stent System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f8a190ec9912cb17eb90132438d0017 and manufactured by ANGIOMED GMBH & CO. MEDIZINTECHNIK KG. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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